Validation Engineer; Lab Equipment

Senior Recruitment Consultant at Panda International | Placing top talent at leading Life Sciences companies

Validation Engineer (Lab Equipment) | Leading Global Biotech Manufacturer

A leading global biotech manufacturer in Switzerland is seeking a Lab Equipment Specialist to support engineering, maintenance, and laboratory qualification activities within a GMP-regulated environment.

This junior-level position focuses on CQV activities, equipment qualification, documentation, and compliance support across a wide range of laboratory systems.

You will collaborate closely with Engineering, QA, QC, Validation, Operations, and external suppliers to ensure equipment readiness and lifecycle compliance.

• Support CQV activities for laboratory equipment.
• Execute installation, qualification, and operational phases for lab instruments
  .
• Coordinate with cross-functional teams for equipment release
  .
• Support documentation for deviations, CAPAs, change controls
  , and lifecycle activities.
• Collaborate with suppliers for qualification and technical assessments
  .
• Ensure compliance with internal procedures and requirements
  .
• Maintain and update internal SOPs
  .

• Execute and review validation documents:
  URS, DQ, IQ, OQ, PQ
  .
• Support GxP impact assessments for new or modified equipment.
• Coordinate and follow up on SAT activities
  .
• Provide technical support on compliance and equipment lifecycle topics.
• Contribute to continuous improvement initiatives
  .

• Degree in Life Sciences, Engineering, Chemistry, Biotech
  , or equivalent.
• Background as a Lab Technician or experience in QA/QC is accepted.
• CQV / Validation training or certification is a plus.

• Experience in CQV or Validation in pharma or biotech environments.
• Hands‑on experience in GxP laboratories or regulated production settings.
• Strong understanding of GxP/GRP
  , data integrity, and equipment lifecycle.
• Experience working with laboratory equipment (e.g.,
  HPLC, UHPLC, centrifuges, incubators
  ).
• Familiar with deviations, CAPA, risk assessments, change controls
  .
• Previous experience with the same end‑client (non‑mandatory).

• Strong organizational skills and priority management
  .
• Excellent communication and customer‑oriented mindset
  .
• Ability to work independently and in a team
  .

• Fluent in French and English
  .
• Comfortable with digital tools; experience with Val Genesis or CARA is a plus.

Start Date: ASAP

Functional Area: Engineering & Skilled Trade

Interested? Apply or send your CV to Miguel Gomes at or contact .

• Mid‑Senior level

• Contract

• Biotechnology Research and Pharmaceutical Manufacturing

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